Radical emulsion polymerizations of vinylcyclopropanes, 1,1-bis(ethoxycarbonyl)-2-vinylcyclopropane (ECVCP) and 1,1-dichloro-2-vinylcyclopropane (CVCP) were examined. ECVCP underwent soap-free and soap-in emulsion polymerizations satisfactorily to afford the ring-opened polymer in good yields. Polym
Synthesis and radical ring-opening polymerization of vinylcyclopropanes bearing vinylsilane groups
โ Scribed by Fumio Sanda; Junji Murata; Takeshi Endo
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- English
- Weight
- 147 KB
- Volume
- 36
- Category
- Article
- ISSN
- 0887-624X
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โฆ Synopsis
Synthesis and radical polymerization of novel vinylcyclopropanes; 1-carboethoxy-2-trimethylsilyl-2-vinylcyclopropane (1a) and 1-carboethoxy-2-(1-trimethylsilyl)-vinylcyclopropane (1b), were examined. 1a and 1b were prepared by the coupling reaction of 2-trimethylsilylbutadiene with ethyl diazoacetate, which was prepared from glycine ethyl ester hydrochloride. The radical polymerization of 1a and 1b was carried out at 60ยฐC in bulk for 40 h in the presence of 2,2ะ-azobis(isobutyronitrile) (5 mol % vs. monomer). Poly(1) consisted of a 1,5-ring-opened unit. Desilylation reaction of poly(1) proceeded quantitatively in aqueous hydrochloric acid.
๐ SIMILAR VOLUMES
Radical polyadditions of vinylcyclopropane having spiroacetal moiety, 1, 10divinyl-4,8,12,15-tetraoxatrispiro[2.2.2.2.2.2]pentadecane ( 1), and various dithiols were examined. 1 was prepared by the reaction of 1,1-dichloro-2-vinylcyclopropane and pentaerythritol, and radical polyadditions of 1 and d
Syntheses and radical ring-opening polymerizations of vinylcyclopropanone derivertives having cyclic six-membered acetal, exomethylene, and phenyl groups; 1vinyl-6-methylene-4,8-dioxaspiro[2.5]octane ( 2b), 1-vinyl-5,7-dimethyl-6-methylene-4,8-dioxaspiro[2.5]octane ( 2c), 1-vinyl-5-phenyl-4,8-dioxas